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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 908670Generated: October 30, 2026

HCID 67392406, compound → HCID 44476497, compound

https://huagongshe.com/reaction/908670

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 67392406HCID 67392406—
ReactantHCID 67392639HCID 67392639—
SolventEthanolHCID 702—
ProductHCID 44476497HCID 444764979%

Reaction Conditions

Temperature60 °C

Reaction Steps

5-({3-[(3-aminopropyl)(methyl)amino]propyl}amino)-2-methyl-1,3-benzothiazole-4,7-dione is solubilized in 250 ml of ethanol and 2.12 g (6.16 mmol; 0.8 equivalent) of 5-methoxy-N-(4-methoxyphenyl)-4,7-dioxo-4,7-dihydro-1,3-benzothiazole-2-carboxamide is added. The reaction mixture is maintained under stirring at 60° C. for 4 hours, then the solvent is evaporated off under reduced pressure. The residue is then purified by chromatography on a silica column (eluent: dichloromethane/methanol: 95/5) and 450 mg (yield=9%) of N-(4-methoxyphenyl)-5-{[3-(methyl{3-[(2-methyl-4,7-dioxo-4,7-dihydro-1,3-benzothiazol-5-yl)amino]propyl}amino)propyl]amino}-4,7-dioxo-4,7-dihydro-1,3-benzothiazole-2-carboxamide is obtained in the form of red powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08017637B2
Source datasetuspto-grants-2011_09
ORD IDord-2fbccc395f3a4f5a8bd725df1048cb9b
Source noteuspto-grants-2011_09